CRISPR-based biosensing is prospective for rapid and sensitive diagnosis of pediatric tuberculosis

Chunyang Lyu1, Hua Shi1, Yali Cui1

  • 1Department of Laboratory Medicine, West China Second Hospital, Sichuan University, Chengdu, Sichuan, China; Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu, Sichuan, China.

Insights

Diagnosing pediatric tuberculosis (TB) is difficult. CRISPR-based biosensing platforms offer a sensitive, rapid, and cost-effective solution for early detection and treatment guidance in children.

Area of Science:

  • Molecular Biology
  • Biotechnology
  • Infectious Diseases

Background:

  • Pediatric tuberculosis (TB) diagnosis is challenging due to non-specific symptoms and low bacterial load in samples.
  • Current diagnostic methods for childhood TB lack sensitivity, speed, and cost-effectiveness, hindering global control efforts.
  • A critical need exists for advanced diagnostic tools to improve pediatric TB detection and management.

Purpose of the Study:

  • To highlight the potential of CRISPR-based biosensing platforms for diagnosing pediatric tuberculosis.
  • To advocate for further research evaluating CRISPR platforms in pediatric specimens, particularly noninvasive samples.
  • To explore the utility of CRISPR platforms for drug resistance identification and genotyping in pediatric TB.

Main Methods:

  • Leveraging the specific and rapid Cas-protein-based catalytic activities of CRISPR systems.
  • Utilizing CRISPR-based biosensing platforms for the detection of nucleic acid traces from Mycobacterium tuberculosis.
  • Focusing on the sensitivity, speed, and cost-effectiveness of CRISPR platforms in preliminary assessments.

Main Results:

  • CRISPR platforms demonstrate superior sensitivity in detecting pathogen nucleic acid traces compared to conventional methods.
  • These platforms offer significant advantages in terms of time and cost savings for diagnostic applications.
  • Preliminary findings suggest high potential for CRISPR platforms in identifying drug resistance and performing genotyping.

Conclusions:

  • CRISPR-based biosensing platforms show significant promise as a sensitive, rapid, and low-cost tool for pediatric TB diagnosis.
  • Further clinical validation in pediatric populations, especially using noninvasive specimens, is warranted.
  • Successful implementation of CRISPR platforms can facilitate early diagnosis, guide appropriate treatment, and support the WHO End-TB strategy.